Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder.

Manhattan plot of OCD GWAS meta-analysis.The y-axis represents –log10 P-values (two-sided, not adjusted for multiple testing) for the association of variants with OCD using an inverse-variance weighted fixed effects model (ncases = 53,660 and ncontrols = 2,044,417). The x-axis shows chromosomes 1 to 22. The horizontal red line represents the threshold for genome-wide significance (P = 5 × 10−8). Index variants of genome-wide significant loci are highlighted as a green diamond.

Gene-based, tissue, and cell type enrichment analyses.a, List of 25 genes that were implicated in at least two of the five different gene-based tests (significance indicated by grey dots) and passed the TWAS colocalization and/or SMR-HEIDI filters (significance indicated by orange dots). Conditionally independent genes within each locus are indicated by blue dots. b, Enrichment of OCD GWAS signal in human brain-related tissues from GTEx (v8). No significant enrichment was observed in the peripheral tissues (not included in the figure). The horizontal bar size represents the significance of the enrichment measured using the MAGMA gene set enrichment test or partitioned LDSC. c, Top 20 groups of brain cell types (n = 35 total tested) enriched with OCD GWAS signal using MAGMA. Dots represent –log10 P-values from MAGMA gene set enrichment tests of individual neuronal cell types from Zeisel et al.30. Vertical crosses represent the mean −log10 P-value observed for each brain cell type group. Blue crosses represent a significant enrichment of OCD GWAS signals (false discovery rate across 35 groups, FDR < 0.05), while pink crosses indicate non-significant enrichment. Grey points represent the association (−log10 P-value) for each single cell cluster (“level 5” analysis defined by Zeisel et al.30) in a given cell type (e.g., excitatory neurons, cerebral cortex).

Genetic correlations (rG) between OCD and 112 phenotypes.This includes psychiatric, substance use, cognition/socioeconomic status (SES), personality, psychological, neurological, autoimmune, cardiovascular, anthropomorphic/diet, fertility, and other phenotypes. References and sample sizes of the corresponding summary statistics of the GWAS studies can be found in Supplementary Table 18. The OCD summary statistics are of the main meta-analysis (ncases = 53,660 and ncontrols = 2,044,417). Error bars represent the 95% confidence intervals for the genetic correlation estimates (rG). Red circles indicate significant associations with a P-value adjusted for multiple testing with the Benjamini-Hochberg procedure to control the FDR (< 0.05). Black circles indicate associations that are not significant.